碳酸乙烯酯
电解质
碳酸二甲酯
热分解
溶解
阳极
锂(药物)
碳酸盐
无机化学
材料科学
化学
石墨
化学工程
有机化学
电极
物理化学
甲醇
内分泌学
工程类
医学
作者
Koeun Kim,Inbok Park,Se‐Young Ha,Yeonkyoung Kim,Myung-Heuio Woo,Myung-Hwan Jeong,Woo Cheol Shin,Makoto Ue,Sung You Hong,Nam‐Soon Choi
标识
DOI:10.1016/j.electacta.2016.12.126
摘要
The cycling and storage performances of LiCoO2 (LCO)-LiNi0.5Co0.2Mn0.3O2 (NCM)/pitch-coated silicon alloy-graphite (Si-C) full cells with ethylene carbonate (EC)–based and fluoroethylene carbonate (FEC)–based electrolytes are investigated at elevated temperatures. Excess FEC (used as a co-solvent in LiPF6-based electrolytes), which is not completely consumed during the formation of the solid electrolyte interphase (SEI) layer on the electrodes, is prone to defluorination in the presence of Lewis acids such as PF5; this reaction can generate unwanted HF and various acids (H3OPF6, HPO2F2, H2PO3F, H3PO4) at elevated temperatures. Our investigation reveals that the HF and acid compounds that are formed by FEC decomposition causes significant dissolution of transition metal ions (from the LCO-NCM cathode) into the electrolyte at elevated temperatures; as a result, the reversible capacity of the full cells reduces because of the deposition of the dissolved metal ions onto the anode. Moreover, we demonstrate possible mechanisms that account for the thermal instability of FEC in LiPF6-based electrolytes at elevated temperatures using model experiments.
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